| Literature DB >> 6741550 |
K Aoyama, K Terashima, Y Imai, N Katsushima, Y Okuyama, K Niikawa, T Mukada, K Takahashi.
Abstract
The present paper deals with immunohistochemical and ultrastructural study of the lymph nodes of sinus histiocytosis with massive lymphadenopathy (Rosai and Dorfman, SHML) of a 12-year-old Japanese boy. This is the fourth case in Japan. Osseous manifestation was also found in the bilateral ulnae. With hallmarks of S-100 protein and interdigitating cytoplasmic extensions, the phagocytizing histiocytes proliferating in the sinuses were considered to be derived mostly from interdigitating cells in the paracortex or T cell dependent area, which have heretofore been regarded as nonphagocytizing. Furthermore, it is most interesting that lymphoid cells bearing thymic cortical cell-antigen (OKT 6) were increasingly recognized in the patient's peripheral blood. These results suggested that SHML is a specialized reactive histiocytosis analogous to histiocytosis X and histiocytic medullary reticulosis.Entities:
Mesh:
Year: 1984 PMID: 6741550 DOI: 10.1111/j.1440-1827.1984.tb07565.x
Source DB: PubMed Journal: Acta Pathol Jpn ISSN: 0001-6632